Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0264356
Disease: Childhood bronchiectasis
Childhood bronchiectasis 		1 0 1 0.25 0 0
CUI: C2751288
Disease: Neutropenia, Severe Congenital, Autosomal Dominant 2
Neutropenia, Severe Congenital, Autosomal Dominant 2 		1 0 1 0.25 0 0
CUI: C3671688
Disease: Cyclic Hematopoesis
Cyclic Hematopoesis 		1 0 1 0.25 0 0
CUI: C4049241
Disease: Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency
Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency 		1 0 1 0.25 0 0
CUI: C4290088
Disease: decreased absolute neurophile count (ANC)
decreased absolute neurophile count (ANC) 		1 0 1 0.25 0 0
CUI: C0271407
Disease: Synchysis scintillans
Synchysis scintillans 		2 0 1 0.20 0 0
CUI: C0272167
Disease: Reticular dysgenesis
Reticular dysgenesis 		2 0 1 0.20 0 0
CUI: C1274789
Disease: Ligneous conjunctivitis
Ligneous conjunctivitis 		2 0 1 0.20 0 0
CUI: C1842930
Disease: Neutropenia, Nonimmune Chronic Idiopathic, Adult
Neutropenia, Nonimmune Chronic Idiopathic, Adult 		2 0 1 0.20 0 0
CUI: C1850127
Disease: Osteopetrosis, Autosomal Recessive 1
Osteopetrosis, Autosomal Recessive 1 		2 0 1 0.20 0 0
CUI: C4551971
Disease: Albers-Schonberg Disease, Autosomal Recessive
Albers-Schonberg Disease, Autosomal Recessive 		2 0 1 0.20 0 0
CUI: C0272175
Disease: Immune neutropenia
Immune neutropenia 		3 0 1 0.17 0 0
CUI: C0432261
Disease: Osteopetrosis - intermediate type
Osteopetrosis - intermediate type 		3 0 1 0.17 0 0
CUI: C0855999
Disease: Abnormal eosinophil morphology
Abnormal eosinophil morphology 		3 0 1 0.17 0 0
CUI: C1698818
Disease: Photodamaged skin
Photodamaged skin 		3 0 1 0.17 0 0
CUI: C1850083
Disease: Irregular ossification at anterior rib ends
Irregular ossification at anterior rib ends 		3 0 1 0.17 0 0
CUI: C1850134
Disease: Sandwich appearance of vertebral bodies
Sandwich appearance of vertebral bodies 		3 0 1 0.17 0 0
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
Plasminogen Deficiency, Type I 		3 0 1 0.17 0 0
CUI: C1969093
Disease: Osteopetrosis, Autosomal Recessive 6
Osteopetrosis, Autosomal Recessive 6 		3 0 1 0.17 0 0
CUI: C3839957
Disease: Hereditary cystatin C amyloid angiopathy
Hereditary cystatin C amyloid angiopathy 		3 0 1 0.17 0 0
CUI: C0853697
Disease: Neutrophil count decreased
Neutrophil count decreased 		4 5 1 0.14 1 3.3E-02
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		4 0 1 0.14 0 0
CUI: C1858673
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 		4 0 1 0.14 0 0
CUI: C4021624
Disease: Osteosclerosis of the base of the skull
Osteosclerosis of the base of the skull 		4 0 1 0.14 0 0
CUI: C4024763
Disease: Optic atrophy from cranial nerve compression
Optic atrophy from cranial nerve compression 		4 0 1 0.14 0 0